Species

KNApSAcK Entry

Organism name Dalbergia spp.
Genus Dalbergia
Family Fabaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Dalbergia
Linked NCBI taxonomy ID 53862
Linked level genus

Family

Family in NCBI taxonomy Fabaceae
ID 3803

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class rosids
ID 71275

Metabolite list (9)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
KCF-S
cluster
phytochemical
cluster
figure
C00002576 External link 512 Shekanin
/ Shekkanin
/ Tectoridin
/ Tectorigenin 7-O-glucoside
CHEMBL520214
C120040
0 / 2 No. 2 No. 15
C00002509 External link 512 Betavulgarin
/ 2'-Hydroxy-5-methoxy-6,7-methylenedioxyisoflavone
No. 27 No. 15
C00010193 External link 512 Methyldalbergin
/ 6,7-Dimethoxy-4-phenylcoumarin
No. 54 No. 17
C00009715 External link 512 (+-)-Mucronulatol
/ 7,3'-Dihydroxy-2',4'-dimethoxyisoflavan
CHEMBL253474
CHEMBL478971
CHEMBL1087024
5 / 1 / 0 No. 73 No. 15
C00010261 External link 512 Obtusaquinol
/ (R,S)-2,5-Dihydroxy-4-methoxydalbergiquinol
CHEMBL465608
No. 977
C00010264 External link 512 (R)-5-Hydroxy-2,4-dimethoxydalbergiquinol
CHEMBL252862
CHEMBL451345
No. 977
C00010253 External link 512 (S)-4'-Hydroxy-4-methoxydalbergione
CHEMBL255296
CHEMBL1374504
6 / 4 / 4 No. 1327 No. 18
C00002549 External link 512 (R)-4-Methoxydalbergione
CHEMBL255297
CHEMBL466581
CHEMBL1554531
18 / 23 / 57 No. 1327 No. 18
C00010254 External link 512 (S)-4,4'-Dimethoxydalbergione
CHEMBL1436980
14 / 11 / 10 No. 1327 No. 18

Human Protein / Gene in interactions

25 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P16050 Arachidonate 15-lipoxygenase Enzyme C00002549 C00010253 C00010254 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002549 C00010253 C00010254 0 / 1
P10636 Microtubule-associated protein tau Unclassified protein C00002549 C00010253 C00010254 4 / 3
O15296 Arachidonate 15-lipoxygenase B Enzyme C00002549 C00010253 C00010254 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00002549 C00010253 C00010254 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002549 C00010253 C00010254 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00002549 C00010254 1 / 1
Q9UBT6 DNA polymerase kappa Enzyme C00002549 C00010254 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00002549 C00010254 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00002549 C00010254 2 / 3
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00002549 C00010254 0 / 0
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00002549 C00010254 2 / 2
P04637 Cellular tumor antigen p53 Transcription Factor C00002549 7 / 37
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002549 3 / 3
P28482 Mitogen-activated protein kinase 1 Erk C00010254 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00009715 0 / 0
P18054 Arachidonate 12-lipoxygenase, 12S-type Enzyme C00010254 2 / 0
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00009715 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00009715 0 / 0
O75496 Geminin Unclassified protein C00009715 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00009715 1 / 0
O00255 Menin Unclassified protein C00002549 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00002549 1 / 2
Q13951 Core-binding factor subunit beta Unclassified protein C00002549 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00002549 1 / 4

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (25)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#114500 Colorectal cancer; crc P18054
#119900 Digital clubbing, isolated congenital P15428
#133239 Esophageal cancer P04637
P18054
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 O75874
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#211980 Lung cancer P04637
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (57)

KEGG name UniProt
H00033 Adrenal carcinoma O00255 (related)
P04637 (related)
H00034 Carcinoid O00255 (related)
H00045 Malignant islet cell carcinoma O00255 (related)
H00246 Primary hyperparathyroidism O00255 (related)
H01102 Pituitary adenomas O00255 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
Q01196 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
H00006 Hairy-cell leukemia P04637 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
H00013 Small cell lung cancer P04637 (related)
H00014 Non-small cell lung cancer P04637 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
H00016 Oral cancer P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P04637 (related)
P04637 (marker)
H00018 Gastric cancer P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00022 Bladder cancer P04637 (related)
H00025 Penile cancer P04637 (related)
P04637 (marker)
H00026 Endometrial Cancer P04637 (related)
H00027 Ovarian cancer P04637 (related)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
H00042 Glioma P04637 (related)
P04637 (marker)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00055 Laryngeal cancer P04637 (related)
P04637 (marker)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (marker)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)

Diseases related to CTD interactions

2 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D056486 Drug-Induced Liver Injury C00002576
D005234 Fatty Liver C00002576